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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
TQ0146 | Ac-DEVD-CHO | Apoptosis , Caspase | |
Ac-DEVD-CHO is a specific Caspase-3 inhibitor (Ki: 230 pM).Ac-DEVD-CHO has an inhibitory effect in SLNT-induced apoptosis. | |||
TQ0146L | Ac-DEVD-CHO acetate | Caspase-3 Inhibitor I,N-acetyl-asp-glu-val-asp-al,Ac-DEVD-CHO acetate (169332-60-9 free base) | Caspase |
Caspase-3 Inhibitor I (N-acetyl-asp-glu-val-asp-al) is a specific inhibitor of Caspase-3. | |||
T41069 | CHO-C-PEG2-C-CHO | CHO-C-PEG2-C-CHO | |
CHO-C-PEG2-C-CHO is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system ... | |||
T21617 | MG-115 | Z-LL-Nva-CHO | Proteasome |
MG-115 (Z-LL-Nva-CHO) is a potent and reversible inhibitor of proteasome , with K i s of 21 nM and 35 nM for 20S and 26S proteasome, respectively. MG-115 specifically inhibit the chymotrypsin-like activity of the proteas... | |||
T78640 | Z-LLF-CHO | Z-Leu-Leu-Phe-CHO | Proteasome |
Z-LLF-CHO (Z-Leu-Leu-Phe-CHO) effectively inhibits the chymotrypsin-like activity of the pituitary multicatalytic proteinase complex with a Ki value of 460 nM. Additionally, this compound serves as an inhibitor of NF-κB ... | |||
T80531 | Ac-AAVALLPAVLLALLAP-DEVD-CHO | DEVD-CHO-CPP 32 | Caspase |
Ac-AAVALLPAVLLALLAP-DEVD-CHO (DEVD-CHO-CPP 32) serves as a potent and reversible inhibitor of caspase-3 [1]. | |||
T39722 | CHO-CH2-PEG1-CH2-Boc | CHO-CH2-PEG1-CH2-Boc | |
CHO-CH2-PEG1-CH2-Boc is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome sys... | |||
T80624 | Ac-VAD-CHO | Ac-Val-Ala-Asp-CHO | Caspase |
Ac-Val-Ala-Asp-CHO (Ac-VAD-CHO) serves as a pan-caspase inhibitor and preserves mitochondrial membrane potential (MMP) while preventing the release of cytochrome c in cells subjected to hypoxia [1]. | |||
T83205 | Ac-DNLD-CHO | Ac-Asp-Asn-Leu-Asp-CHO | Caspase |
Ac-DNLD-CHO (Ac-Asp-Asn-Leu-Asp-CHO) is an inhibitor of Caspase-3/7, exhibiting IC50 values of 9.89 nM and 245 nM, and approximate Ki values of 0.68 nM and 55.7 nM, respectively. This compound is utilized in the study of... | |||
T80735 | Z-Gly-Pro-Phe-Leu-CHO | Z-GPFL-CHO | Proteasome |
Z-Gly-Pro-Phe-Leu-CHO (Z-GPFL-CHO) is a tetrapeptide aldehyde serving as a selective and potent proteasome inhibitor, demonstrating inhibition constants (Ki) of 1.5 µM, 2.3 µM, and 40.5 µM for branched-chain amino acid-p... | |||
T78586L | Ac-IETD-CHO TFA | Ac-IETD-CHO TFA(191338-86-0 Free base ) | Apoptosis , Caspase |
Ac-IETD-CHO TFA is a granzyme B and caspase-8 inhibitor that inhibits caspase8 activity by blocking caspase3 precursor cleavage.Ac-IETD-CHO TFA inhibits Fas-mediated apoptosis. | |||
T41236 | Z-FY-CHO | ||
Z-FY-CHO (Z-Phe-Tyr-CHO) is a specific and potent cathepsin L (CTSL) inhibitor [1] [2]. | |||
T2154 | MG-132 | Z-LLL-al,Z-Leu-Leu-Leu-CHO | Apoptosis , Proteasome , Autophagy |
MG-132 (Z-Leu-Leu-Leu-al) is a 26S proteasome inhibitor (IC50=100 nM) that is cell-permeable and reversible. MG-132 acts as an autophagy activator and also induces apoptosis. | |||
T36350 | Cho-Arg (trifluoroacetate salt) | ||
Cho-Arg is a steroid-based cationic lipid that contains a cholesterol skeleton coupled to an L-arginine head group. It forms a complex with plasmid DNA and decreases plasmid DNA migration in an agarose-gel retardant assa... | |||
T29233 | Z-LLNle-CHO | ||
Z-LLNle-CHO is a cell permeable inhibitor of gamma-secretase. Z-LLNle-CHO induces apoptosis of human glioblastoma tumor-initiating cells by proteasome inhibition and mitotic arrest response. | |||
T36368 | 2H-Cho-Arg (trifluoroacetate salt) | ||
2H-Cho-Arg is a steroid-based cationic lipid that contains a 2H-cholesterol skeleton coupled to an L-arginine head group and can be used to facilitate gene transfection. It forms a complex with plasmid DNA (pDNA) and dec... | |||
T6583 | MG-101 | ALLN,Ac-LLnL-CHO,Calpain inhibitor I,Calpain inhibitor-1,MG101 | Cysteine Protease , Proteasome |
MG-101 (Calpain inhibitor I) is a cell-permeable and potent inhibitor of cysteine proteases including calpains and lysosomal cathepsins. | |||
T19883 | Ac-YVAD-CHO | L 709049,L-709049,L709049 | |
L 709049 is a biologically active compound that is a selective inhibitor of interleukin-1β converting enzyme (Caspase-1). Caspase inhibitors interfere with the initiation of apoptosis and have multiple clinical applicati... | |||
T80513 | YVAD-CHO | ||
YVAD-CHO is an inhibitor of interleukin-1β converting enzyme (ICE, caspase 1) that has been shown to partially mitigate motoneuron death in mice with lesioned facial nerves [1]. | |||
T80093 | IETD-CHO TFA | Caspase | |
IETD-CHO TFA (Caspase-8-IN-1) functions as a potent inhibitor of caspase-8 [1]. |